Forceps Epilation Angled

GUDID 05060480400139

BLINK MEDICAL LIMITED

Dressing/utility forceps, tweezers-like, single-use

• Primary Device ID: 05060480400139
• NIH Device Record Key: 9cf704fc-c3c0-4b53-9927-19a8dfe186dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Forceps Epilation Angled
• Version Model Number: HR131
• Company DUNS: 738288096
• Company Name: BLINK MEDICAL LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060480400139 [Package]; Contains: 05060480405769; Package: [10 Units]; In Commercial Distribution
GS1	05060480405769 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-29
• Device Publish Date: 2024-05-21

On-Brand Devices [Forceps Epilation Angled]

• 05060480407145: 10-1300
• 05060480400139: HR131